D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Immunology D-index 47 Citations 11,907 114 World Ranking 3455 National Ranking 297

Overview

What is she best known for?

The fields of study she is best known for:

  • Immune system
  • Cytokine
  • Internal medicine

Catharien M. U. Hilkens mainly investigates Immunology, Cytokine, Interleukin 12, Cell biology and T cell. Immunology is frequently linked to Cellular differentiation in her study. Her work carried out in the field of Cytokine brings together such families of science as Endocrinology, Immune system, Immunotherapy and Antigen.

Her Interleukin 12 research includes elements of CD40 and Antigen-presenting cell. Her research in Cell biology intersects with topics in Prostaglandin E2, Gene and Cell growth. The T cell study which covers Secretion that intersects with Mesenchymal stem cell, Clonogenic assay and Cell therapy.

Her most cited work include:

  • T-cell priming by type-1 and type-2 polarized dendritic cells: the concept of a third signal. (898 citations)
  • IL-12-deficient dendritic cells, generated in the presence of prostaglandin E2, promote type 2 cytokine production in maturing human naive T helper cells. (555 citations)
  • IRF4 Transcription Factor-Dependent CD11b+ Dendritic Cells in Human and Mouse Control Mucosal IL-17 Cytokine Responses (554 citations)

What are the main themes of her work throughout her whole career to date?

The scientist’s investigation covers issues in Immunology, T cell, Cytokine, Cell biology and Immune system. Her study involves Immune tolerance, Dendritic cell, Arthritis, Antigen and Immunotherapy, a branch of Immunology. Her work on IL-2 receptor as part of general T cell study is frequently linked to Population, therefore connecting diverse disciplines of science.

Her work in Cytokine addresses subjects such as Antigen-presenting cell, which are connected to disciplines such as Interleukin 4. Her Cell biology research incorporates themes from CD40, Phenotype, Stimulation, T-cell receptor and Interleukin 12. Her Immune system research incorporates elements of Inflammation and Cell.

She most often published in these fields:

  • Immunology (95.31%)
  • T cell (38.28%)
  • Cytokine (22.66%)

What were the highlights of her more recent work (between 2017-2021)?

  • Immunology (95.31%)
  • Arthritis (21.88%)
  • Population (18.75%)

In recent papers she was focusing on the following fields of study:

Immunology, Arthritis, Population, T cell and Immune tolerance are her primary areas of study. Her Gene signature research extends to the thematically linked field of Immunology. Her Gene signature research is multidisciplinary, incorporating perspectives in Whole blood, CD40, Downregulation and upregulation, CD8 and Initial therapy.

Her Arthritis research is multidisciplinary, incorporating elements of Epitope and IL-2 receptor. The various areas that Catharien M. U. Hilkens examines in her Immune tolerance study include Clinical trial and Transplantation. Her research integrates issues of Cell activation, Cytokine secretion and Inflammatory arthritis in her study of Antigen.

Between 2017 and 2021, her most popular works were:

  • Macrophage proliferation distinguishes 2 subgroups of knee osteoarthritis patients. (29 citations)
  • Macrophage proliferation distinguishes 2 subgroups of knee osteoarthritis patients. (29 citations)
  • Minimum Information about T Regulatory Cells: A Step toward Reproducibility and Standardization. (25 citations)

In her most recent research, the most cited papers focused on:

  • Immune system
  • Gene
  • Cytokine

Catharien M. U. Hilkens mostly deals with CD86, Cancer research, Transplantation, Cell therapy and Macrophage. Catharien M. U. Hilkens interconnects Whole blood, CD40, Interferon, Downregulation and upregulation and CD8 in the investigation of issues within CD86. Her Cancer research study combines topics from a wide range of disciplines, such as Inflammation, Proliferation Marker, Macrophage proliferation and Pathogenesis.

Her work deals with themes such as Chimeric antigen receptor, Immunotherapy and Neuroscience, which intersect with Transplantation. The Cell therapy study combines topics in areas such as Clinical trial, Bioinformatics and Immune tolerance.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

T-cell priming by type-1 and type-2 polarized dendritic cells: the concept of a third signal.

Pawel Kaliński;Catharien M.U Hilkens;Eddy A Wierenga;Martien L Kapsenberg.
Immunology Today (1999)

1290 Citations

IRF4 Transcription Factor-Dependent CD11b+ Dendritic Cells in Human and Mouse Control Mucosal IL-17 Cytokine Responses

Andreas Schlitzer;Naomi McGovern;Pearline Teo;Teresa Zelante.
Immunity (2013)

786 Citations

IL-12-deficient dendritic cells, generated in the presence of prostaglandin E2, promote type 2 cytokine production in maturing human naive T helper cells.

P. Kalinski;C.M.U. Hilkens;A. Snijders;F.G.M. Snijdewint.
Journal of Immunology (1997)

734 Citations

α-Type-1 Polarized Dendritic Cells A Novel Immunization Tool with Optimized CTL-inducing Activity

Robbie B. Mailliard;Anna Wankowicz-Kalinska;Quan Cai;Amy Wesa.
Cancer Research (2004)

604 Citations

Prostaglandin E2 Induces the Final Maturation of IL-12-Deficient CD1a+CD83+ Dendritic Cells: The Levels of IL-12 Are Determined During the Final Dendritic Cell Maturation and Are Resistant to Further Modulation

Paweł Kaliński;Joost H. N. Schuitemaker;Catharien M. U. Hilkens;Martien L. Kapsenberg.
Journal of Immunology (1998)

562 Citations

High-level IL-12 production by human dendritic cells requires two signals.

Alies Snijders;Pawel Kalinski;Catharien M. U. Hilkens;Martien L. Kapsenberg.
International Immunology (1998)

521 Citations

Adult Human Fibroblasts Are Potent Immunoregulatory Cells and Functionally Equivalent to Mesenchymal Stem Cells

Muzlifah A. Haniffa;Xiao-Nong Wang;Udo Holtick;Michelle Rae.
Journal of Immunology (2007)

431 Citations

Human Dendritic Cells Require Exogenous Interleukin-12–Inducing Factors to Direct the Development of Naive T-Helper Cells Toward the Th1 Phenotype

C.M.U. Hilkens;P. Kalinski;M. de Boer;M.L. Kapsenberg.
Blood (1997)

402 Citations

Final maturation of dendritic cells is associated with impaired responsiveness to IFN-gamma and to bacterial IL-12 inducers: decreased ability of mature dendritic cells to produce IL-12 during the interaction with Th cells

Paweł Kaliński;Joost H. N. Schuitemaker;Catharien M. U. Hilkens;Eddy A. Wierenga.
Journal of Immunology (1999)

399 Citations

Frailty and the role of inflammation, immunosenescence and cellular ageing in the very old: Cross-sectional findings from the Newcastle 85+ Study

Joanna Collerton;Carmen Martin-Ruiz;Karen Davies;Catharien M. Hilkens.
Mechanisms of Ageing and Development (2012)

397 Citations

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